U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 100

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6953176copy number variation1nstd229human GRCh38 chr14: 20,015,858-20,044,820 , GRCh37.p13 chr14: 20,484,017-20,512,979 OR4U1P, OR4K13
    nsv6950973copy number variation1nstd229human GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 OR4L1, RNA5SP382, 25 more genes
    nsv6491381copy number variation1nstd223human GRCh38 chr14: 20,043,194-20,043,471 , GRCh37.p13 chr14: 20,511,353-20,511,630 OR4U1P
    nsv6487981copy number variation1nstd223human GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 RNA5SP382, OR4L1, 25 more genes
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6290645copy number variation1nstd102humanUncertain significance GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 OR4T1P, OR11G1P, 25 more genes
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv6030492copy number variation1nstd212human GRCh38 chr14: 20,037,880-20,042,646 , GRCh37.p13 chr14: 20,506,039-20,510,805 OR4U1P
    nsv5943393copy number variation1nstd209human GRCh38 chr14: 20,038,752-20,231,884 , GRCh37.p13 chr14: 20,506,911-20,700,043 PSMB7P1, OR11G2, 12 more genes
    nsv4994065copy number variation1nstd200human GRCh38 chr14: 20,038,750-20,129,722 , GRCh37.p13 chr14: 20,506,909-20,597,881 OR4L1, OR4K17, 3 more genes
    nsv4994064copy number variation1nstd200human GRCh38 chr14: 20,015,858-20,044,820 , GRCh37.p13 chr14: 20,484,017-20,512,979 OR4U1P, OR4K13
    nsv4994063copy number variation1nstd200human GRCh38 chr14: 20,013,868-20,436,718 , GRCh37.p13 chr14: 20,482,027-20,904,877 OR4K17, OR4L1, 25 more genes
    nsv4845095copy number variation1nstd200human GRCh37 chr14: 20,484,017-20,512,979 , GRCh38.p12 chr14: 20,015,858-20,044,820 OR4U1P, OR4K13
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4455321copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,511,672-21,174,548 , GRCh38.p12 chr14: 20,043,513-20,706,389 PARP2, TRL-AAG2-3, 53 more genes
    nsv4455170copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,511,672-20,903,963 , GRCh38.p12 chr14: 20,043,513-20,435,804 OR11G2, KLHL33, 22 more genes
    nsv4417741copy number variation1nstd174human GRCh37 chr14: 20,511,673-20,698,504 , GRCh38.p12 chr14: 20,043,514-20,230,345 OR4U1P, OR4N5, 12 more genes
    nsv4386449copy number variation1nstd173human GRCh37 chr14: 20,511,673-20,539,350 , GRCh38.p12 chr14: 20,043,514-20,071,191 OR4L1, OR4U1P
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center